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2,3,4,5,6-pentakis(propionyloxy)cyclohexyl propionate is a complex organic compound with the molecular formula C21H31O7. It is characterized by a cyclohexyl ring with five propionyloxy groups (ester groups derived from propionic acid) attached at positions 2, 3, 4, 5, and 6, and a propionate group at the first position. This molecule is known for its potential applications in various chemical and industrial processes, such as the synthesis of polymers and the production of certain pharmaceuticals. Due to its unique structure, it can also be used as a building block in the creation of more complex molecules. The compound's properties, such as solubility and reactivity, can be influenced by the presence of these functional groups, making it a versatile component in chemical research and development.

5776-50-1

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5776-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5776-50-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5776-50:
(6*5)+(5*7)+(4*7)+(3*6)+(2*5)+(1*0)=121
121 % 10 = 1
So 5776-50-1 is a valid CAS Registry Number.

5776-50-1Downstream Products

5776-50-1Relevant academic research and scientific papers

An extremely efficient and green method for the acylation of secondary alcohols, phenols and naphthols with a deep eutectic solvent as the catalyst

Nguyen, Hai Truong,Tran, Phuong Hoang

, p. 98365 - 98368 (2016/10/31)

The typical deep eutectic solvent [CholineCl][ZnCl2]3, easily prepared from choline chloride and zinc chloride, is green and useful for the acylation of secondary alcohols, phenols, and naphthols with acid anhydrides. Its efficiency allows the acylation of sterically hindered secondary alcohols and acid anhydrides to proceed in high yield under mild condition. The catalyst is cheap, easy to handle, conveniently synthesized in a single step, and recyclable for several times without significant loss of catalytic activity.

The oxidation of partially acylated myoinositols

Kurzer, Frederick,Chapman, Dennis

, p. 68 - 78 (2007/10/03)

1,3,4,6-Tetrakis-and 1,3,4,5,6-pentakis-acylmyoinositols are obtained by the controlled catalyzed acylation of myoinositol. The extent of the substitution depends both on the reaction conditions and the structure of the acylating agent, including steric f

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